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CAS

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1191415-40-3

2-(2,2-dichlorovinyl)benzenethiol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1191415-40-3 Structure

  • Basic information

    1. Product Name: 2-(2,2-dichlorovinyl)benzenethiol
    2. Synonyms: 2-(2,2-dichlorovinyl)benzenethiol
    3. CAS NO:1191415-40-3
    4. Molecular Formula:
    5. Molecular Weight: 205.108
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1191415-40-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(2,2-dichlorovinyl)benzenethiol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(2,2-dichlorovinyl)benzenethiol(1191415-40-3)
    11. EPA Substance Registry System: 2-(2,2-dichlorovinyl)benzenethiol(1191415-40-3)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1191415-40-3(Hazardous Substances Data)

1191415-40-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1191415-40-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,1,4,1 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1191415-40:
(9*1)+(8*1)+(7*9)+(6*1)+(5*4)+(4*1)+(3*5)+(2*4)+(1*0)=133
133 % 10 = 3
So 1191415-40-3 is a valid CAS Registry Number.

1191415-40-3Relevant articles and documents

Intramolecular cross-coupling of gem-dibromoolefins: A mild approach to 2-bromo benzofused heterocycles

Newman, Stephen G.,Aureggi, Valentina,Bryan, Christopher S.,Lautens, Mark

supporting information; experimental part, p. 5236 - 5238 (2010/01/31)

Highly useful halogenated benzofurans and benzothiophenes are prepared from readily available gem-dibromoolefins using a mild, ligand-free copper catalyzed cross-coupling procedure.

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